Evidence map›Paper›PMID 35243294›Full record

ArticleMaterials today. Bio2022

A metastasis-on-a-chip approach to explore the sympathetic modulation of breast cancer bone metastasis.

Francisco Conceição, Daniela M Sousa, Joshua Loessberg-Zahl, Anke R Vollertsen, Estrela Neto, Kent Søe, Joana Paredes, Anne Leferink, Meriem Lamghari

Open access · goldAbstract read
In one paragraph

Article in Materials today. Bio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Cancer metastasisFrontiers in bioengineering and biotechnology · 2026
    Review
  5. Review
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  8. Microphysiological systems for metastasis research: a stepwise approach.Cellular oncology (Dordrecht, Netherlands) · 2025
    Review
  9. Review
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  11. Article
  12. Review
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  16. Article
  17. Article
  18. Review
  19. Review
  20. Tumor-on-chip platforms for breast cancer continuum concept modeling.Frontiers in bioengineering and biotechnology · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Francisco ConceiçãoInstituto de Investigação e Inovação Em Saúde (I3S), Universidade Do Porto, 4200-135, Porto, Portugal.
Daniela M SousaInstituto de Investigação e Inovação Em Saúde (I3S), Universidade Do Porto, 4200-135, Porto, Portugal.
Joshua Loessberg-ZahlBIOS Lab on a Chip Group, MESA+ Institute for Nanotechnology, Max Planck - University of Twente Center for Complex Fluid Dynamics, University of Twente, P.O. Box 217, 7500, AE Enschede, the Netherlands.
Anke R VollertsenApplied Stem Cell Technologies, TechMed Centre, University of Twente, PO Box 217, 7500, AE, Enschede, the Netherlands.
Estrela NetoInstituto de Investigação e Inovação Em Saúde (I3S), Universidade Do Porto, 4200-135, Porto, Portugal.
Kent SøeClinical Cell Biology, Vejle Hospital/Lillebaelt Hospital, Department of Regional Health Research, University of Southern Denmark, 7100, Vejle, Denmark.
Joana ParedesInstituto de Investigação e Inovação Em Saúde (I3S), Universidade Do Porto, 4200-135, Porto, Portugal.
Anne LeferinkApplied Stem Cell Technologies, TechMed Centre, University of Twente, PO Box 217, 7500, AE, Enschede, the Netherlands.
Meriem LamghariInstituto de Investigação e Inovação Em Saúde (I3S), Universidade Do Porto, 4200-135, Porto, Portugal.
Universidade do Porto · PTUniversity of Twente · NLMax Planck University of Twente Center for Complex Fluid Dynamics · NLUniversity of Southern Denmark · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organ-on-a-chip models have emerged as a powerful tool to model cancer metastasis and to decipher specific crosstalk between cancer cells and relevant regulators of this particular niche. Recently, the sympathetic nervous system (SNS) was proposed as an important modulator of breast cancer bone metastasis. However, epidemiological studies concerning the benefits of the SNS targeting drugs on breast cancer survival and recurrence remain controversial. Thus, the role of SNS signaling over bone metastatic cancer cellular processes still requires further clarification. Herein, we present a novel humanized organ-on-a-chip model recapitulating neuro-breast cancer crosstalk in a bone metastatic context. We developed and validated an innovative three-dimensional printing based multi-compartment microfluidic platform, allowing both selective and dynamic multicellular paracrine signaling between sympathetic neurons, bone tropic breast cancer cells and osteoclasts. The selective multicellular crosstalk in combination with biochemical, microscopic and proteomic profiling show that synergistic paracrine signaling from sympathetic neurons and osteoclasts increase breast cancer aggressiveness demonstrated by augmented levels of pro-inflammatory cytokines (e.g. interleukin-6 and macrophage inflammatory protein 1α). Overall, this work introduced a novel and versatile platform that could potentially be used to unravel new mechanisms involved in intracellular communication at the bone metastatic niche.

Indexed as

Bone metastasisBreast cancerIL-6, interleukin 6IL, interleukinMCP-1, monocyte chemoattractant protein 1Metastasis-on-a-chipMIP-1α, macrophage inflammatory protein 1αNE, norepinephrineParacrinePDMS, poly-dimethylsiloxaneSNS, Sympathetic Nervous SystemSympathetic nervous systemTH, tyrosine hydroxylase

Identifiers

PMID35243294
PMCPMC8857466
OpenAlexW4212839638

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.